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Prion protein interaction with the C-terminal SH3 domain of Grb2 studied using NMR and optical spectroscopy
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
title
Prion protein interaction with the C-terminal SH3 domain of Grb2 studied using NMR and optical spectroscopy
(English)
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
main subject
SH3 domain
0 references
prion protein family
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Prion protein
1 reference
stated in
GOA release 2020-03-11
Growth factor receptor bound protein 2
1 reference
stated in
GOA release 2020-03-11
spectroscopy
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author
Kurt Wüthrich
series ordinal
2
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author name string
Dominikus A. Lysek
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
language of work or name
English
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publication date
17 August 2004
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stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
published in
Biochemistry
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
volume
43
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
page(s)
10393–10399
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
issue
32
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
cites work
Cellular prion protein promotes Brucella infection into macrophages
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Molecular modelling indicates that the pathological conformations of prion proteins might be beta-helical.
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
The program XEASY for computer-supported NMR spectral analysis of biological macromolecules
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Membrane-targeting of signalling molecules by SH2/SH3 domain-containing adaptor proteins
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Cellular functions regulated by Src family kinases
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
PrPC directly interacts with proteins involved in signaling pathways
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Analysis of 27 mammalian and 9 avian PrPs reveals high conservation of flexible regions of the prion protein
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
A single amino acid alteration (101L) introduced into murine PrP dramatically alters incubation time of transmissible spongiform encephalopathy
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Solution structure of Grb2 reveals extensive flexibility necessary for target recognition
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Processing of multi-dimensional NMR data with the new software PROSA
1 reference
stated in
COCI
retrieved
9 October 2022
reference URL
https://opencitations.net/index/coci/api/v1/references/10.1021/BI0494828
Identifiers
DOI
10.1021/BI0494828
0 references
PubMed ID
15301538
1 reference
stated in
PubMed
PubMed ID
15301538
retrieved
24 January 2017
ResearchGate publication ID
8408730
0 references
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